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More informationSummary record - 98th meeting of the Pharmaceutical Committee (20 January 2022)
Advice to sponsors on managing the impact of the war in Ukraine on clinical trials
EMA establishes Cancer Medicines Forum with academia to optimise cancer treatments in clinical practice
Public Consultation open on: ICH guideline Q14 on analytical procedure development
The European Medicines Agency has published ICH guideline Q2(R2) on validation of analytical procedures for public consultation.
In March FDA published 'An Acceptable Circular of Information for the Use of Human Blood and Blood Components' - Guidance for Industry
Medicines: get scientific advice from MHRA - New Email Address
This Roadmap Tool sets out the key steps and activities in the end-to-end pathway for Advanced Therapy Medicinal Products (ATMPs) in England from non-clinical research through to treatment provision & monitoring.
CTIS newsflash #07 - 18 March 2022
Meeting highlights from the Committee for Veterinary Medicinal Products (CVMP) 15-16 March 2022